Canonical Allele Identifier: CA1314900

Gene: PTPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198728437G>A , CM000663.2:g.198728437G>A	GRCh38
NC_000001.10:g.198697566G>A , CM000663.1:g.198697566G>A	GRCh37
NC_000001.9:g.196964189G>A	NCBI36
NG_007730.1:g.94342G>A
NG_007730.2:g.94343G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491302.2:n.871G>A
ENST00000697630.1:n.5648G>A
ENST00000697631.1:c.1533G>A	ENSP00000513363.1:p.Lys511=
ENST00000697632.1:c.780G>A	ENSP00000513364.1:p.Lys260=
ENST00000697633.1:c.293G>A
ENST00000348564.11:c.1335G>A	ENSP00000306782.7:p.Lys445=
ENST00000442510.8:c.1818G>A MANE Select	ENSP00000411355.3:p.Lys606=
ENST00000348564.10:c.1335G>A	ENSP00000306782.7:p.Lys445=
ENST00000367367.8:c.1620G>A	ENSP00000356337.5:p.Lys540=
ENST00000442510.6:c.1818G>A	ENSP00000411355.3:p.Lys606=
ENST00000529828.5:c.1674G>A	ENSP00000469141.1:p.Lys558=
ENST00000530727.5:c.1476G>A	ENSP00000433536.2:p.Lys492=
NM_002838.4:c.1818G>A	NP_002829.3:p.Lys606=
NM_080921.3:c.1335G>A	NP_563578.2:p.Lys445=
XM_006711472.2:c.1674G>A	XP_006711535.1:p.Lys558=
XM_006711473.2:c.1620G>A	XP_006711536.1:p.Lys540=
XM_006711474.2:c.1476G>A	XP_006711537.1:p.Lys492=
XM_006711472.4:c.1674G>A	XP_006711535.1:p.Lys558=
XM_006711473.3:c.1620G>A	XP_006711536.1:p.Lys540=
XM_006711474.3:c.1476G>A	XP_006711537.1:p.Lys492=
NM_002838.5:c.1818G>A MANE Select	NP_002829.3:p.Lys606=
NM_080921.4:c.1335G>A	NP_563578.2:p.Lys445=